| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189441133-189441517 | Common:2; Rare:120 | ||||
| chr2:189783965-189784078 | Common:2; Rare:38 | ||||
| chr2:189784289-189784537 | Common:4; Rare:89; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190534659-190534846 | Common:1; Rare:61 | ||||
| chr2:190880568-190880887 | Common:4; Rare:107 | ||||
| chr2:191014143-191014333 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677856-191678140 | Common:4; Rare:79 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197499783-197500451 | Common:2; Rare:255; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515780-197516102 | Common:2; Rare:111 | ||||
| chr2:197705221-197705396 | Common:1; Rare:68 | ||||
| chr2:199911080-199911417 | Rare:109 | ||||
| chr2:200510060-200510141 | Rare:21 | ||||
| chr2:200811408-200811589 | Common:1; Rare:60 | ||||
| chr2:200864228-200864252 | Rare:7 |